| Literature DB >> 26628208 |
Shuxiao Zhang1, Wei Wang2, Juan Li3, Ke Cheng3, Jingjing Zhou4, Dan Zhu5, Deyu Yang6, Zihong Liang7, Liang Fang6, Li Liao1, Peng Xie8.
Abstract
CD36 is a member of the class B scavenger receptor family of cell surface proteins, which plays a major role in fatty acid, glucose and lipid metabolism. Besides, CD36 functions as a microglial surface receptor for amyloid beta peptide. Regarding this, we suggest CD36 might also contribute to neuropsychiatric disease. The aim of this study was to achieve a behavioral phenotype of CD36 knockout (CD36(-/-)) mice. We characterized the behavior of CD36(-/-) mice and C57BL/6J mice by subjecting them to a series of tests, which include SHIRPA primary behavioral screen test, 1% sucrose preference test, elevated plus-maze test, open-field test and forced swimming test. The results showed that CD36(-/-) mice traversed more squares, emitted more defecation, exhibited higher tail elevation and had more aggressive behaviors than C57BL/6J mice. The CD36(-/-) mice spent more time and traveled longer distance in periphery zone in the open-field test. Meanwhile, the numbers that CD36(-/-) mice entered in the open arms of elevated plus-maze were reduced. These findings suggest that CD36(-/-) mice present an anxious phenotype and might be involved in neuropsychiatric disorders.Entities:
Keywords: Anxiety; Behavioral phenotype; CD36 knockout mice; SHIRPA primary screen
Mesh:
Substances:
Year: 2015 PMID: 26628208 DOI: 10.1016/j.bbr.2015.11.027
Source DB: PubMed Journal: Behav Brain Res ISSN: 0166-4328 Impact factor: 3.332